Condición
Atrial fibrillation
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Variantes que influyen en Atrial fibrillation según las pruebas clínicas
Las clasificaciones de pruebas clínicas están diseñadas para ayudar a los médicos a comprender cómo los cambios genéticos, conocidos como variantes, podrían afectar la salud de una persona y guiar las decisiones médicas. Las variantes se etiquetan como Causantes de Enfermedad (dañinas), Probablemente Causantes de Enfermedad, Efecto Desconocido (impacto desconocido), Probablemente Sin Efecto (probablemente no dañinas) y Sin Efecto (no dañinas). Esta clasificación se basa en una combinación de antecedentes familiares, pruebas de laboratorio y predicciones por computadora para determinar el impacto de las variantes.
Variantes que afectan tanto a hombres como a mujeres biológicas
Genotype
C
C
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters C/G has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
G
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
C
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters C/G has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
G
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters G/G has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
C
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
T
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters C/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
T
T
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
C
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
The genotype with the letters C/C has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
C
T
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters C/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
T
T
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
The genotype with the letters T/T has no effect on your disease risk. Carriers of this genetic result are usually not at risk of developing the disease.
Genotype
A
A
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
No available data
Genotype
A
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
No available data
Genotype
G
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
No available data
Genotype
A
A
Level of evidence
Sin efecto
Unisex
1 Sources
Participants: 0
No available data
Genotype
A
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
No available data
Genotype
G
G
Level of evidence
Efecto desconocido
Unisex
1 Sources
Participants: 0
No available data
Variantes que influyen en Atrial fibrillation según estudios científicos
Las clasificaciones de estudios científicos tienen como objetivo descubrir cómo funcionan las variantes genéticas y su papel en las enfermedades, los rasgos y la evolución. Las variantes se categorizan según su impacto funcional, como pérdida de función (reduce la actividad génica), ganancia de función (aumenta la actividad génica), neutral (sin impacto significativo) o conservación evolutiva. Esta clasificación utiliza datos experimentales, estudios de población y análisis computacionales para comprender los efectos de las variantes. A diferencia de las pruebas clínicas, que se centran en los impactos inmediatos en la salud, los estudios científicos exploran mecanismos genéticos más amplios e implicaciones a largo plazo.
Variantes que afectan tanto a hombres como a mujeres biológicas
Genotype
C
C
Level of evidence
Sin efecto
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Probabilidad aumentada
Unisex
5 Sources
Participants: 1300352
The genotype with the letters C/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
T
T
Level of evidence
Probabilidad aumentada
Unisex
5 Sources
Participants: 1300352
The genotype with the letters T/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
C
C
Level of evidence
Sin efecto
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Probabilidad aumentada
Unisex
5 Sources
Participants: 1300352
The genotype with the letters C/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
T
T
Level of evidence
Probabilidad aumentada
Unisex
5 Sources
Participants: 1300352
The genotype with the letters T/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
C
C
Level of evidence
Sin efecto
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Probabilidad aumentada
Unisex
6 Sources
Participants: 5158915
The genotype with the letters C/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
T
T
Level of evidence
Probabilidad aumentada
Unisex
6 Sources
Participants: 5158915
The genotype with the letters T/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
C
C
Level of evidence
Sin efecto
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Probabilidad aumentada
Unisex
6 Sources
Participants: 5158915
The genotype with the letters C/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
T
T
Level of evidence
Probabilidad aumentada
Unisex
6 Sources
Participants: 5158915
The genotype with the letters T/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
C
C
Level of evidence
Sin efecto
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Probabilidad aumentada
Unisex
5 Sources
Participants: 5122123
The genotype with the letters C/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
T
T
Level of evidence
Probabilidad aumentada
Unisex
5 Sources
Participants: 5122123
The genotype with the letters T/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
C
C
Level of evidence
Sin efecto
Unisex
0 Sources
Participants: 0
No available data
Genotype
C
T
Level of evidence
Probabilidad aumentada
Unisex
5 Sources
Participants: 5122123
The genotype with the letters C/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.
Genotype
T
T
Level of evidence
Probabilidad aumentada
Unisex
5 Sources
Participants: 5122123
The genotype with the letters T/T is considered a risk factor for developing the disease. Carriers of this genetic result are at increased risk of developing the disease.